Efficient site management is essential for an effective trial and rapid collection of accurate results.

Our CRAs are highly-trained and available 24/7. They are adept at building long-term partnerships with investigators and supporting efficient trial recruitment, as well as ensuring proper data quality and consistency.

Throughout the study, our team provides support in areas, including:

• site personnel training and education
• study drug and non-drug supplies logistics
• tracking regulatory document revisions
• tracking protocol deviations
• tracking subject status within the trial